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Homocysteine and Dementia: An International Consensus Statement(1)

Identification of modifiable risk factors provides a crucial approach to the prevention of dementia. Nutritional or nutrient-dependent risk factors are especially important because dietary modifications or use of dietary supplements may lower the risk factor level. One such risk factor is a raised c...

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Autores principales: Smith, A. David, Refsum, Helga, Bottiglieri, Teodoro, Fenech, Michael, Hooshmand, Babak, McCaddon, Andrew, Miller, Joshua W., Rosenberg, Irwin H., Obeid, Rima
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5836397/
https://www.ncbi.nlm.nih.gov/pubmed/29480200
http://dx.doi.org/10.3233/JAD-171042
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author Smith, A. David
Refsum, Helga
Bottiglieri, Teodoro
Fenech, Michael
Hooshmand, Babak
McCaddon, Andrew
Miller, Joshua W.
Rosenberg, Irwin H.
Obeid, Rima
author_facet Smith, A. David
Refsum, Helga
Bottiglieri, Teodoro
Fenech, Michael
Hooshmand, Babak
McCaddon, Andrew
Miller, Joshua W.
Rosenberg, Irwin H.
Obeid, Rima
author_sort Smith, A. David
collection PubMed
description Identification of modifiable risk factors provides a crucial approach to the prevention of dementia. Nutritional or nutrient-dependent risk factors are especially important because dietary modifications or use of dietary supplements may lower the risk factor level. One such risk factor is a raised concentration of the biomarker plasma total homocysteine, which reflects the functional status of three B vitamins (folate, vitamins B12, B6). A group of experts reviewed literature evidence from the last 20 years. We here present a Consensus Statement, based on the Bradford Hill criteria, and conclude that elevated plasma total homocysteine is a modifiable risk factor for development of cognitive decline, dementia, and Alzheimer’s disease in older persons. In a variety of clinical studies, the relative risk of dementia in elderly people for moderately raised homocysteine (within the normal range) ranges from 1.15 to 2.5, and the Population Attributable risk ranges from 4.3 to 31%. Intervention trials in elderly with cognitive impairment show that homocysteine-lowering treatment with B vitamins markedly slows the rate of whole and regional brain atrophy and also slows cognitive decline. The findings are consistent with moderately raised plasma total homocysteine (>11 μmol/L), which is common in the elderly, being one of the causes of age-related cognitive decline and dementia. Thus, the public health significance of raised tHcy in the elderly should not be underestimated, since it is easy, inexpensive, and safe to treat with B vitamins. Further trials are needed to see whether B vitamin treatment will slow, or prevent, conversion to dementia in people at risk of cognitive decline or dementia.
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spelling pubmed-58363972018-03-07 Homocysteine and Dementia: An International Consensus Statement(1) Smith, A. David Refsum, Helga Bottiglieri, Teodoro Fenech, Michael Hooshmand, Babak McCaddon, Andrew Miller, Joshua W. Rosenberg, Irwin H. Obeid, Rima J Alzheimers Dis Editorial Identification of modifiable risk factors provides a crucial approach to the prevention of dementia. Nutritional or nutrient-dependent risk factors are especially important because dietary modifications or use of dietary supplements may lower the risk factor level. One such risk factor is a raised concentration of the biomarker plasma total homocysteine, which reflects the functional status of three B vitamins (folate, vitamins B12, B6). A group of experts reviewed literature evidence from the last 20 years. We here present a Consensus Statement, based on the Bradford Hill criteria, and conclude that elevated plasma total homocysteine is a modifiable risk factor for development of cognitive decline, dementia, and Alzheimer’s disease in older persons. In a variety of clinical studies, the relative risk of dementia in elderly people for moderately raised homocysteine (within the normal range) ranges from 1.15 to 2.5, and the Population Attributable risk ranges from 4.3 to 31%. Intervention trials in elderly with cognitive impairment show that homocysteine-lowering treatment with B vitamins markedly slows the rate of whole and regional brain atrophy and also slows cognitive decline. The findings are consistent with moderately raised plasma total homocysteine (>11 μmol/L), which is common in the elderly, being one of the causes of age-related cognitive decline and dementia. Thus, the public health significance of raised tHcy in the elderly should not be underestimated, since it is easy, inexpensive, and safe to treat with B vitamins. Further trials are needed to see whether B vitamin treatment will slow, or prevent, conversion to dementia in people at risk of cognitive decline or dementia. IOS Press 2018-02-20 /pmc/articles/PMC5836397/ /pubmed/29480200 http://dx.doi.org/10.3233/JAD-171042 Text en © 2018 – IOS Press and the authors. All rights reserved https://creativecommons.org/licenses/by-nc/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Non-Commercial (CC BY-NC 4.0) License (https://creativecommons.org/licenses/by-nc/4.0/) , which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Editorial
Smith, A. David
Refsum, Helga
Bottiglieri, Teodoro
Fenech, Michael
Hooshmand, Babak
McCaddon, Andrew
Miller, Joshua W.
Rosenberg, Irwin H.
Obeid, Rima
Homocysteine and Dementia: An International Consensus Statement(1)
title Homocysteine and Dementia: An International Consensus Statement(1)
title_full Homocysteine and Dementia: An International Consensus Statement(1)
title_fullStr Homocysteine and Dementia: An International Consensus Statement(1)
title_full_unstemmed Homocysteine and Dementia: An International Consensus Statement(1)
title_short Homocysteine and Dementia: An International Consensus Statement(1)
title_sort homocysteine and dementia: an international consensus statement(1)
topic Editorial
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5836397/
https://www.ncbi.nlm.nih.gov/pubmed/29480200
http://dx.doi.org/10.3233/JAD-171042
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